Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002006.2 | 1637 | Missense Mutation | CGG,TGG | R526W | NP_001002006.1 |
NM_001199086.1 | 1637 | Missense Mutation | CGG,TGG | R509W | NP_001186015.1 |
NM_001199087.1 | 1637 | Missense Mutation | CGG,TGG | R543W | NP_001186016.1 |
NM_001199088.1 | 1637 | Missense Mutation | CGG,TGG | R528W | NP_001186017.1 |
NM_033253.3 | 1637 | Missense Mutation | CGG,TGG | R466W | NP_150278.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199103.1 | 1637 | Intron | NP_001186032.1 | ||
NM_001199104.1 | 1637 | Missense Mutation | CGG,TGG | R526W | NP_001186033.1 |